Bibliographic Details
Title: |
Induction of Hepatitis E Virus Anti-ORF3 Antibodies from Systemic Administration of a Muscle-Specific Adeno-Associated Virus (AAV) Vector |
Authors: |
Lars Maurer, Jihad El Andari, Kleopatra Rapti, Laura Spreyer, Eike Steinmann, Dirk Grimm, Viet Loan Dao Thi |
Source: |
Viruses, Vol 14, Iss 2, p 266 (2022) |
Publisher Information: |
MDPI AG, 2022. |
Publication Year: |
2022 |
Collection: |
LCC:Microbiology |
Subject Terms: |
adeno-associated virus, AAV, hepatitis E virus, HEV, vector-based vaccine, neutralisation, Microbiology, QR1-502 |
More Details: |
The hepatitis E virus (HEV) is a major global health problem, leading to large outbreaks in the developing world and chronic infections in the developed world. HEV is a non-enveloped virus, which circulates in the blood in a quasi-enveloped form. The quasi-envelope protects HEV particles from neutralising anti-capsid antibodies in the serum; however, most vaccine approaches are designed to induce an immune response against the HEV capsid. In this study, we explored systemic in vivo administration of a novel synthetic and myotropic Adeno-associated virus vector (AAVMYO3) to express the small HEV phosphoprotein ORF3 (found on quasi-enveloped HEV) in the musculature of mice, resulting in the robust and dose-dependent formation of anti-ORF3 antibodies. Neutralisation assays using the serum of ORF3 AAV-transduced mice showed a modest inhibitory effect on the infection of quasi-enveloped HEV in vivo, comparable to previously characterised anti-ORF3 antibodies used as a control. The novel AAVMYO3 capsid used in this study can serve as a versatile platform for the continued development of vector-based vaccines against HEV and other infectious agents, which could complement traditional vaccines akin to the current positive experience with SARS-CoV-2. |
Document Type: |
article |
File Description: |
electronic resource |
Language: |
English |
ISSN: |
1999-4915 |
Relation: |
https://www.mdpi.com/1999-4915/14/2/266; https://doaj.org/toc/1999-4915 |
DOI: |
10.3390/v14020266 |
Access URL: |
https://doaj.org/article/59f135ac156247f2869a8a5148203a1d |
Accession Number: |
edsdoj.59f135ac156247f2869a8a5148203a1d |
Database: |
Directory of Open Access Journals |
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